Katecho, Inc. - FDA 510(k) Cleared Devices
Recent clearances: K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85, KM-30 TENS ELECTRODE, K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
26
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Katecho, Inc. General & Plastic Surgery ✕
1 devices